Update (1995) on clinical trials of antiviral therapy and prophylaxis for AIDS-related cytomegalovirus disease.

M A Jacobson
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Abstract

An overview of the current state of antiviral therapy and prophylaxis for opportunistic cytomegalovirus (CMV) disease in 1995 is provided, focusing primarily on therapeutic trials for AIDS-related CMV retinitis. Retinitis is the most common serious CMV end-organ disease in AIDS; and it is the one for which clinical end-points can be measured most objectively and precisely. Standard antiviral chemotherapy for CMV retinitis consists of chronic intravenous treatment with either ganciclovir or foscarnet, each of which significantly delays loss of vision compared to no treatment. New agents such as HPMPC and new treatment strategies such as intravitreal ganciclovir may be more effective than standard treatment in delaying time to retinitis progression but are associated with serious toxicity problems. Preliminary data from a placebo-controlled trial of oral ganciclovir suggest that this agent reduces the risk of developing CMV end-organ disease by 50%; however, the implications of oral ganciclovir prophylaxis for development of antiviral drug resistance are unknown.

关于艾滋病相关巨细胞病毒疾病的抗病毒治疗和预防的临床试验的最新资料(1995年)。
概述了1995年机会性巨细胞病毒(CMV)疾病的抗病毒治疗和预防现状,主要侧重于艾滋病相关巨细胞病毒视网膜炎的治疗试验。视网膜炎是艾滋病患者最常见的严重巨细胞病毒终末器官疾病;它是一种最客观、最精确地衡量临床终点的方法。CMV视网膜炎的标准抗病毒化疗包括慢性静脉注射更昔洛韦或氟膦酸钠,与不治疗相比,每一种治疗都能显著延缓视力丧失。新的药物,如hmpc和新的治疗策略,如玻璃体内注射更昔洛韦,在延缓视网膜炎进展方面可能比标准治疗更有效,但与严重的毒性问题有关。一项口服更昔洛韦的安慰剂对照试验的初步数据表明,该药物可将CMV终末器官疾病的发生风险降低50%;然而,口服更昔洛韦预防抗病毒药物耐药的意义尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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